Canonical Allele Identifier: CA566689260

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31323950-G-GCTGCAGCGTCTCCTTCCCGTT
• gnomAD v4: 6-31356173-G-GCTGCAGCGTCTCCTTCCCGTT
• MyVariant Identifiers: chr6:g.31323950_31323951insCTGCAGCGTCTCCTTCCCGTT (hg19) ; chr6:g.31356173_31356174insCTGCAGCGTCTCCTTCCCGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356175_31356176insGCAGCGTCTCCTTCCCGTTCT , CM000668.2:g.31356175_31356176insGCAGCGTCTCCTTCCCGTTCT	GRCh38
NC_000006.11:g.31323952_31323953insGCAGCGTCTCCTTCCCGTTCT , CM000668.1:g.31323952_31323953insGCAGCGTCTCCTTCCCGTTCT	GRCh37
NC_000006.10:g.31431931_31431932insGCAGCGTCTCCTTCCCGTTCT	NCBI36
NG_023187.1:g.6039_6040insAACGGGAAGGAGACGCTGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2085_2086insAACGGGAAGGAGACGCTGCAG
ENST00000481849.6:n.2085_2086insAACGGGAAGGAGACGCTGCAG
ENST00000497377.6:n.2085_2086insAACGGGAAGGAGACGCTGCAG
ENST00000640094.2:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000491275.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000696558.1:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000512716.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000696559.1:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000512717.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000696560.1:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000512718.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000696561.1:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000512719.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000696562.1:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000512720.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000412585.7:c.612_613insAACGGGAAGGAGACGCTGCAG MANE Select	ENSP00000399168.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000412585.6:c.612_613insAACGGGAAGGAGACGCTGCAG	ENSP00000399168.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
ENST00000434333.1:c.645_646insAACGGGAAGGAGACGCTGCAG	ENSP00000405931.1:p.Glu215_Arg216insAsnGlyLysGluThrLeuGln
ENST00000474381.1:n.487_488insAACGGGAAGGAGACGCTGCAG
ENST00000498007.1:n.878_879insAACGGGAAGGAGACGCTGCAG
NM_005514.6:c.612_613insAACGGGAAGGAGACGCTGCAG	NP_005505.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
XM_011514556.1:c.645_646insAACGGGAAGGAGACGCTGCAG	XP_011512858.1:p.Glu215_Arg216insAsnGlyLysGluThrLeuGln
XM_011514557.1:c.612_613insAACGGGAAGGAGACGCTGCAG	XP_011512859.1:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
XR_926175.1:n.622_623insAACGGGAAGGAGACGCTGCAG
NM_005514.7:c.612_613insAACGGGAAGGAGACGCTGCAG	NP_005505.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln
NM_005514.8:c.612_613insAACGGGAAGGAGACGCTGCAG MANE Select	NP_005505.2:p.Glu204_Arg205insAsnGlyLysGluThrLeuGln